US2927053A - Method of destroying fungi employing alkoxybenzyl alkanol amines - Google Patents
Method of destroying fungi employing alkoxybenzyl alkanol amines Download PDFInfo
- Publication number
- US2927053A US2927053A US614363A US61436356A US2927053A US 2927053 A US2927053 A US 2927053A US 614363 A US614363 A US 614363A US 61436356 A US61436356 A US 61436356A US 2927053 A US2927053 A US 2927053A
- Authority
- US
- United States
- Prior art keywords
- alkoxybenzyl
- alkanol amines
- destroying fungi
- employing
- fungi employing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 10
- 241000233866 Fungi Species 0.000 title claims description 6
- 150000001412 amines Chemical class 0.000 title description 2
- 125000006307 alkoxy benzyl group Chemical group 0.000 title 1
- 239000000203 mixture Substances 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 10
- 230000000855 fungicidal effect Effects 0.000 claims description 7
- 239000000417 fungicide Substances 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 238000009472 formulation Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 4
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 4
- 229910003446 platinum oxide Inorganic materials 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 241000213004 Alternaria solani Species 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- -1 e.g. Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- UBLCRUHXSMDNQZ-UHFFFAOYSA-N 2-[(4-methoxyphenyl)methylamino]ethanol Chemical compound COC1=CC=C(CNCCO)C=C1 UBLCRUHXSMDNQZ-UHFFFAOYSA-N 0.000 description 1
- 235000006810 Caesalpinia ciliata Nutrition 0.000 description 1
- 241000059739 Caesalpinia ciliata Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- RJMUSRYZPJIFPJ-UHFFFAOYSA-N niclosamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C=C1Cl RJMUSRYZPJIFPJ-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/08—Amines; Quaternary ammonium compounds containing oxygen or sulfur
- A01N33/10—Amines; Quaternary ammonium compounds containing oxygen or sulfur having at least one oxygen or sulfur atom directly attached to an aromatic ring system
Definitions
- Illustrative specific compounds of the above type are the compounds having the structure 2- (p-methoxybenzylamino) ethanol 3 -(p-methoxybenzylamino -propanol Compounds of the above type are useful in a number of applications such as biologically active materials in formulations adopted for use as fungicides as well as in other uses.
- the materials can be prepared by combining an alkanolamine such as ethanolamine or S-amino propanol, with anisaldehyde and catalytically hydrogenating this mixture.
- Initial reactionto remove water desirably. is carried out in an organic solvent, e.g., benzene, at an elevated temperature.
- the benzene is removed and the mixture catalytically hydrogenated using a catalyst such as platinum oxide (Pt with vacum distillation or other separation means to recover the desired product.
- a catalyst such as platinum oxide (Pt with vacum distillation or other separation means to recover the desired product.
- EXAMPLE I Part A water is collected in a water separator. Benzene is then removed by distillation at atmospheric pressure. One half the thus-treated material is catalytically hydrogenated by dissolving it in 250 m1. of methanol and adding 1.0 gm. platinum oxide (PtO Catalytic hydrogenation is carried out at an initial hydrogen pressure of 65 p.s.i.g.,
- Y conidia of Alternaria solani per ml. and held at 100% relative. humidity for 24 hours at 70 F. and are then disease control based on the number of lesions obtained on the control plant-i Following this procedure, it is observed that at the concentrations 6f 2000 and 400 ppm, respectively, the product of Part A is efiective in obtaining a 98% and disease control, respectively, thus indicating a high degree of fungicidal effectiveness.
- Example II Part B is repeated using the product of Example II, Part A at a concentration of 4000 p.p.m. A 79% disease control is observed, thus indicating a high degree of fungicidal efiectiveness.
- Compounds of this invention exhibit biological activity as heretofore shown. These compounds are to be em-"'" ployed in a variety of formulations both liquid and solid including finely-divided powders, granular materials, as well as those liquid solutions, concentrates, emulsifiable concentrates, slurries, and the like, depending upon the application intended and the formulation media employed.
- the compounds used in this invention form biologically active materials which can be employed as an essential ingredient in various compositions which may include such-diluents, extenders, fillers, conditioners, solvents and the like as various clays, diatomaceous earth, talc, spent catalyst, alumina silica materials and such liquids as water and various organic liquids such as acetone, kerosene, benzene, toluene, xylene, 'andother petroleum distillate fractions or mixtures thereof.
- various compositions may include such-diluents, extenders, fillers, conditioners, solvents and the like as various clays, diatomaceous earth, talc, spent catalyst, alumina silica materials and such liquids as water and various organic liquids such as acetone, kerosene, benzene, toluene, xylene, 'andother petroleum distillate fractions or mixtures thereof.
- the method of controlling fungus growth which comprises applying as a fungicide a composition containing as an essential active ingredient a compound having the formula CmOQCmNH-R wherein R is a terminal hydroxy substituted lower alkyl group.
- the method of controlling fungus growth which comprises applying as a fungicide a composition containing as an essential active ingredient a compound having the formula cmoomNH-oalorrlorr 3.v
- the method of controlling fungus growth which comprises applying as a fungicide a composition containing as an essential active ingredient a compound having the formula 1 a References Cited in the file of this patent -UNITED STATES PATENTS 2,430,722 Ladd etal, Nov. 11, 1947 2,545,498 -Sonder1i et al. Mar. 20, 1951 2,574,620 Carlsson Nov. 13, 1951 2,626,227 Lambrech Jan. 20, 1953 2,683,744 Kerwin et a1. July 13, 1954 OTHER REFERENCES Engelhardt et al.: J. Am. Chem. Soc., 72, 2718-2722 1950
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
METHOD OF DESTROYING FUNGI EMPLOYING ALKOXYBENZYL ALKANOL AMINES Janie! S. Eden, Akron, Ohio, assigns: t l'itmnond Alkali Company, Cleveland, Dine, at eor oi-atien'of Delaware No Drawing. Application October s, 1956 Serial No. 614,363
3 Claims. (Cl. 167-30) This invention relates to novel alkditybenzyl alkanolamines.
compounds having the structure wherein R is a hydroxy alkyl group such as CH,CH =OH or CH CH CH -OH. Illustrative specific compounds of the above type are the compounds having the structure 2- (p-methoxybenzylamino) ethanol 3 -(p-methoxybenzylamino -propanol Compounds of the above type are useful in a number of applications such as biologically active materials in formulations adopted for use as fungicides as well as in other uses.
The materials can be prepared by combining an alkanolamine such as ethanolamine or S-amino propanol, with anisaldehyde and catalytically hydrogenating this mixture. Initial reactionto remove water desirably. is carried out in an organic solvent, e.g., benzene, at an elevated temperature. The benzene is removed and the mixture catalytically hydrogenated using a catalyst such as platinum oxide (Pt with vacum distillation or other separation means to recover the desired product.
In order that those skilled in the art may more completely understand the present invention and the preferred methods by which the same may be carried into effect, the following specific examples are offered:
EXAMPLE I (Part A) water is collected in a water separator. Benzene is then removed by distillation at atmospheric pressure. One half the thus-treated material is catalytically hydrogenated by dissolving it in 250 m1. of methanol and adding 1.0 gm. platinum oxide (PtO Catalytic hydrogenation is carried out at an initial hydrogen pressure of 65 p.s.i.g.,
the pressure decreasing to 22.5 p.s.i.g. at the end of the hydrogenation. Methanol is then removed by distillation at atmospheric pressure and the product is vacuum distilled at 145 --147 C. at 2-2.3 mm. Hg to yield a color less oil weighing 147 gm.
More specifically the present invention relates to novel 2,927,053 H l aten ted Mar. 1, 1960 chemical analysis ofthis product indicates preparation of the desired C H NO and is as follows:
Element Percent; Peroeiit Actual Calculated The zap-merhexybenzylami methanol thus pre ared has a refractive inde'ii'.- of 1.5461 at 20 C. x
To illustrate the biological activity of the product "of Part A; fungicidal test's'are conducted against early to mato blight fungus Alternaria solani. .In this procedure; the product of Part A is employed as aqueous fofmu= lations at concentrations of 2000 and 400 p.p.m., rs'pc= tively (using 5% acetone and 0.01% Triton X-l55 (alkyl aryl polyether alcohol) as an emulsifier) These formulations are applied to growing tomato plants (var. Boiiny Best), 5 to 7 inches tall. These formulations are sprayed on the plants and allowed to dry; comparable untreated plants are sprayed with the same formulation, less the toxic-ant. .The thus-treated plants are then sprayed with a spore suspension containing approximately 20,000
Y: conidia of Alternaria solani per ml. and held at 100% relative. humidity for 24 hours at 70 F. and are then disease control based on the number of lesions obtained on the control plant-i Following this procedure, it is observed that at the concentrations 6f 2000 and 400 ppm, respectively, the product of Part A is efiective in obtaining a 98% and disease control, respectively, thus indicating a high degree of fungicidal effectiveness.
EXAMPLE II (Part A) PREPARATION OF B-(p-METHOXYBENZYLAMINO)- PROPANOL A mixture of 75 gm. (1 mol) of 3-aminopropanol, 136
gm. (1 mol) of anisaldehyde and 300 ml. of benzene is refluxed under a water separator for 3 hours until 19 ml. of water is collected. The benzene is then removed by distillation at atmospheric pressure. One-half the thusprepared mixture is subjected to catalytic hydrogenation using 1.0 gm. of platinum oxide (PtO as catalyst and 250 ml. of methanol, initially adjusting the hydrogen pressure to 65 p.s.i.g. Hydrogenation proceeds until the pressure reaches 23 p.s.i.g.
Following catalytic hydrogenation, the platinum oxide (PtO is removed and the methanol separated by distillation. The resultant product is then distilled at 162- 165 C. at 2.53 mm. Hgto obtain a colorless liquid weighing 169 gm. Chemical analysis of thisproduct indicates the formation of the desired C H N0 and is as follows: a
The procedure of Example I, Part B is repeated using the product of Example II, Part A at a concentration of 4000 p.p.m. A 79% disease control is observed, thus indicating a high degree of fungicidal efiectiveness.
Compounds of this invention exhibit biological activity as heretofore shown. These compounds are to be em-"'" ployed in a variety of formulations both liquid and solid including finely-divided powders, granular materials, as well as those liquid solutions, concentrates, emulsifiable concentrates, slurries, and the like, depending upon the application intended and the formulation media employed.
Hence, it will be appreciated that it is contemplated the compounds used in this invention form biologically active materials which can be employed as an essential ingredient in various compositions which may include such-diluents, extenders, fillers, conditioners, solvents and the like as various clays, diatomaceous earth, talc, spent catalyst, alumina silica materials and such liquids as water and various organic liquids such as acetone, kerosene, benzene, toluene, xylene, 'andother petroleum distillate fractions or mixtures thereof. When liquid formulations within the full intended scope of this invention as defined by the appended claims. f
What is claimed is: 1. The method of controlling fungus growth which comprises applying as a fungicide a composition containing as an essential active ingredient a compound having the formula CmOQCmNH-R wherein R is a terminal hydroxy substituted lower alkyl group.
2. The method of controlling fungus growth which comprises applying as a fungicide a composition containing as an essential active ingredient a compound having the formula cmoomNH-oalorrlorr 3.v The method of controlling fungus growth which comprises applying as a fungicide a composition containing as an essential active ingredient a compound having the formula 1 a References Cited in the file of this patent -UNITED STATES PATENTS 2,430,722 Ladd etal, Nov. 11, 1947 2,545,498 -Sonder1i et al. Mar. 20, 1951 2,574,620 Carlsson Nov. 13, 1951 2,626,227 Lambrech Jan. 20, 1953 2,683,744 Kerwin et a1. July 13, 1954 OTHER REFERENCES Engelhardt et al.: J. Am. Chem. Soc., 72, 2718-2722 1950
Claims (1)
1. THE METHOD OF CONTROLLING FUNGUS GROWTH WHICH COMPRISES APPLYING AS A FUNGICIDE A COMPOSITION CONTAINING AS AN ESSENTIAL ACTIVE INGREDIENT A COMPOUND HAVING THE FORMULA
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US614363A US2927053A (en) | 1956-10-08 | 1956-10-08 | Method of destroying fungi employing alkoxybenzyl alkanol amines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US614363A US2927053A (en) | 1956-10-08 | 1956-10-08 | Method of destroying fungi employing alkoxybenzyl alkanol amines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2927053A true US2927053A (en) | 1960-03-01 |
Family
ID=24460937
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US614363A Expired - Lifetime US2927053A (en) | 1956-10-08 | 1956-10-08 | Method of destroying fungi employing alkoxybenzyl alkanol amines |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2927053A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1165930B (en) * | 1961-11-29 | 1964-03-19 | Basf Ag | Fungicides |
| US3227760A (en) * | 1962-07-10 | 1966-01-04 | Velsicol Chemical Corp | N,n-mono- and di-substituted-aralkyl amines |
| US3227756A (en) * | 1962-07-10 | 1966-01-04 | Velsicol Chemical Corp | N,n-mono- and di-substituted-aralkyl amines |
| US3231615A (en) * | 1961-08-19 | 1966-01-25 | Fisons Pest Control Ltd | Tetrachloro-ortho-phenylenediamine and salts thereof |
| US3257274A (en) * | 1960-04-26 | 1966-06-21 | Montedison Spa | Method for killing fungi with betaamino-ethyl ketones |
| US3332998A (en) * | 1963-08-20 | 1967-07-25 | Fisons Pest Control Ltd | 2-nitro-3, 4, 5, 6-tetrachloro-n-aliphetric anilines |
| EP1300402A1 (en) * | 2001-10-04 | 2003-04-09 | Ciba SC Holding AG | Alkoxybenzylamines with antimicrobial properties |
| US20040006061A1 (en) * | 2001-10-04 | 2004-01-08 | Wolfgang Haap | Alkoxybenzylamine |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2430722A (en) * | 1946-04-25 | 1947-11-11 | Us Rubber Co | Derivatives of chlorinated quinones as fungicides |
| US2545498A (en) * | 1947-05-19 | 1951-03-20 | White Lab Inc | 2-[n-(b-dimethylaminomethyl)-n-(4-methoxybenzyl)-amino]-thiazole and process for making same |
| US2574620A (en) * | 1948-04-30 | 1951-11-13 | Recip Ab | Beta-di-piperonyl-amino-ethanol-hydrochloride |
| US2626227A (en) * | 1950-11-30 | 1953-01-20 | Union Carbide & Carbon Corp | 3, 5-dimethylphenoxyethanol, 4-chloro-3, 5-dimethylphenoxyethanol and their use as systemic fungicides for plants |
| US2683744A (en) * | 1953-02-13 | 1954-07-13 | Smith Kline French Lab | Nu-alkoxyalkyl-beta-haloethylamines |
-
1956
- 1956-10-08 US US614363A patent/US2927053A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2430722A (en) * | 1946-04-25 | 1947-11-11 | Us Rubber Co | Derivatives of chlorinated quinones as fungicides |
| US2545498A (en) * | 1947-05-19 | 1951-03-20 | White Lab Inc | 2-[n-(b-dimethylaminomethyl)-n-(4-methoxybenzyl)-amino]-thiazole and process for making same |
| US2574620A (en) * | 1948-04-30 | 1951-11-13 | Recip Ab | Beta-di-piperonyl-amino-ethanol-hydrochloride |
| US2626227A (en) * | 1950-11-30 | 1953-01-20 | Union Carbide & Carbon Corp | 3, 5-dimethylphenoxyethanol, 4-chloro-3, 5-dimethylphenoxyethanol and their use as systemic fungicides for plants |
| US2683744A (en) * | 1953-02-13 | 1954-07-13 | Smith Kline French Lab | Nu-alkoxyalkyl-beta-haloethylamines |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3257274A (en) * | 1960-04-26 | 1966-06-21 | Montedison Spa | Method for killing fungi with betaamino-ethyl ketones |
| US3231615A (en) * | 1961-08-19 | 1966-01-25 | Fisons Pest Control Ltd | Tetrachloro-ortho-phenylenediamine and salts thereof |
| DE1165930B (en) * | 1961-11-29 | 1964-03-19 | Basf Ag | Fungicides |
| US3227760A (en) * | 1962-07-10 | 1966-01-04 | Velsicol Chemical Corp | N,n-mono- and di-substituted-aralkyl amines |
| US3227756A (en) * | 1962-07-10 | 1966-01-04 | Velsicol Chemical Corp | N,n-mono- and di-substituted-aralkyl amines |
| US3332998A (en) * | 1963-08-20 | 1967-07-25 | Fisons Pest Control Ltd | 2-nitro-3, 4, 5, 6-tetrachloro-n-aliphetric anilines |
| EP1300402A1 (en) * | 2001-10-04 | 2003-04-09 | Ciba SC Holding AG | Alkoxybenzylamines with antimicrobial properties |
| US20040006061A1 (en) * | 2001-10-04 | 2004-01-08 | Wolfgang Haap | Alkoxybenzylamine |
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